Canonical Allele Identifier: CA1914326432
Gene: ARID5B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61961364T= , CM000672.2:g.61961364T= GRCh38
NC_000010.10:g.63721123T= , CM000672.1:g.63721123T= GRCh37
NC_000010.9:g.63391129T= NCBI36
NG_030027.1:g.65111T=

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.502+20956T= MANE Select ENSP00000279873.7:n.502+20956T=
ENST00000644638.1:c.502+20956T= ENSP00000494412.1:n.502+20956T=
ENST00000681100.1:c.502+20956T= ENSP00000506119.1:n.502+20956T=
ENST00000279873.11:c.502+20956T= ENSP00000279873.7:n.502+20956T=
NM_032199.2:c.502+20956T= NP_115575.1:n.502+20956T=
XM_011540262.1:c.502+20956T= XP_011538564.1:n.502+20956T=
XM_024448230.1:c.-66+20956T= XP_024303998.1:n.-66+20956T=
NM_032199.3:c.502+20956T= MANE Select NP_115575.1:n.502+20956T=
Search 100 bp 5'
Search 100 bp 3'